IL28B polymorphism is not associated with HCV protease diversity in patients co-infected with HIV and HCV treated with pegylated interferon and ribavirin
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作者:
Osinusi, Anu
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NCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Osinusi, Anu
[1
,2
]
Chary, Aarthi
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机构:
Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
Stanford Univ, Stanford, CA 94305 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Chary, Aarthi
[3
,4
]
Winters, Mark A.
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Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
Stanford Univ, Stanford, CA 94305 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Winters, Mark A.
[3
,4
]
Naggie, Susanna
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机构:
Duke Clin Res Inst, Durham, NC USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Naggie, Susanna
[5
]
Masur, Henry
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NIH, Dept Crit Care Med, Bethesda, MD 20892 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Masur, Henry
[6
]
Polis, Michael A.
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机构:
NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Polis, Michael A.
[2
]
Kottilil, Shyam
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NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USANCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
Kottilil, Shyam
[2
]
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Holodniy, Mark
[3
,4
]
机构:
[1] NCI, CMRP, SAIC Frederick Inc, Frederick, MD 21701 USA
[2] NIAID, Immunoregulat Lab, NIH, Bethesda, MD 20892 USA
[3] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
[4] Stanford Univ, Stanford, CA 94305 USA
[5] Duke Clin Res Inst, Durham, NC USA
[6] NIH, Dept Crit Care Med, Bethesda, MD 20892 USA
Recent studies have demonstrated that IL28B polymorphisms predict therapeutic responses in chronic hepatitis C virus (HCV)-treated patients; however, the effect on HCV viral diversity, particularly on the HCV protease gene, is not clear. This study sought to evaluate the effect of IL28B polymorphisms on HCV diversity at NS3/4 protease region, which may influence therapeutic response to an HCV protease inhibitor based regimen. Twenty-two patients co-infected with HIV and HCV genotype 1, treatment-naive on stable HIV antiretroviral therapy initiating interferon-based treatment were evaluated. Plasma HCV NS3 gene diversity was analyzed by clonal analysis at baseline and end of treatment. IL28B (rs12979860) genotypes were tested for associations with virologic outcomes and diversity parameters. There was similar baseline NS3 diversity in patients with CC (favorable) genotype compared to those with CT/TT (unfavorable) genotypes. There was no significant association between IL28B genotype and baseline NS3 nucleotide p-distance, dS-dN, amino acid p-distance, or nucleotide changes. Among patients without a sustained virologic response, between baseline and follow-up there was a significant trend towards decreased diversity after treatment among patients with favorable genotype, which was not observed in unfavorable genotypes. In patients treated with peginterferon/ribavirin therapy, IL28B polymorphism was not associated with enhanced NS3 diversity at baseline. Among non-SVR patients with the less favorable genotype, there was no change in diversity after treatment. This suggests that IL28B genotype is unlikely to have a negative impact on subsequent HCV PI efficacy in patients co-infected with HIV and HCV patients who have previously failed HCV therapy. J. Med. Virol. 84:15221527, 2012. (c) Published 2012. This article is a U.S. Government work and is in the public domain in the USA.
机构:
Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
De Nicola, S.
Aghemo, A.
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Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
Aghemo, A.
Galmozzi, E.
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Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
Galmozzi, E.
Rumi, M. G.
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机构:
Univ Milan, San Giuseppe Hosp, Hepatol Unit, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
Rumi, M. G.
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D'Ambrosio, R.
De Gasperi, E.
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Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
De Gasperi, E.
Perbellini, R.
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Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, ItalyUniv Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Div Gastroenterol 1, Milan, Italy
机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Dahari, Harel
Markatou, Marianthi
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Markatou, Marianthi
Zeremski, Marija
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Zeremski, Marija
Haller, Ivan
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Haller, Ivan
Ribeiro, Ruy M.
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Ribeiro, Ruy M.
Licholai, Teresa
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Licholai, Teresa
Perelson, Alan S.
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机构:Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA
Perelson, Alan S.
Talal, Andrew H.
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Cornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USACornell Univ, Weill Med Coll, Div Gastroenterol & Hepatol, New York, NY 10021 USA